+Open data
-Basic information
Entry | Database: PDB / ID: 2nv6 | ||||||
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Title | Mycobacterium tuberculosis InhA (S94A) bound with INH-NAD adduct | ||||||
Components | Enoyl-[acyl-carrier-protein] reductase [NADH | ||||||
Keywords | OXIDOREDUCTASE / InhA / S94A / tuberculosis / isoniazid | ||||||
Function / homology | Function and homology information enoyl-[acyl-carrier-protein] reductase activity (NAD(P)H) / trans-2-enoyl-CoA reductase (NADH) activity / mycolic acid biosynthetic process / fatty acid elongation / enoyl-[acyl-carrier-protein] reductase (NADH) / enoyl-[acyl-carrier-protein] reductase (NADH) activity / NAD+ binding / peptidoglycan-based cell wall / fatty acid binding / fatty acid biosynthetic process ...enoyl-[acyl-carrier-protein] reductase activity (NAD(P)H) / trans-2-enoyl-CoA reductase (NADH) activity / mycolic acid biosynthetic process / fatty acid elongation / enoyl-[acyl-carrier-protein] reductase (NADH) / enoyl-[acyl-carrier-protein] reductase (NADH) activity / NAD+ binding / peptidoglycan-based cell wall / fatty acid binding / fatty acid biosynthetic process / response to antibiotic / plasma membrane Similarity search - Function | ||||||
Biological species | Mycobacterium tuberculosis (bacteria) | ||||||
Method | X-RAY DIFFRACTION / SYNCHROTRON / MOLECULAR REPLACEMENT / Resolution: 1.9 Å | ||||||
Authors | Wang, F. / Sacchettini, J.C. | ||||||
Citation | Journal: NAT.MED. (N.Y.) / Year: 2006 Title: Transfer of a point mutation in Mycobacterium tuberculosis inhA resolves the target of isoniazid. Authors: Vilcheze, C. / Wang, F. / Arai, M. / Hazbon, M.H. / Colangeli, R. / Kremer, L. / Weisbrod, T.R. / Alland, D. / Sacchettini, J.C. / Jacobs Jr., W.R. | ||||||
History |
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-Structure visualization
Structure viewer | Molecule: MolmilJmol/JSmol |
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-Downloads & links
-Download
PDBx/mmCIF format | 2nv6.cif.gz | 67 KB | Display | PDBx/mmCIF format |
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PDB format | pdb2nv6.ent.gz | 48.4 KB | Display | PDB format |
PDBx/mmJSON format | 2nv6.json.gz | Tree view | PDBx/mmJSON format | |
Others | Other downloads |
-Validation report
Arichive directory | https://data.pdbj.org/pub/pdb/validation_reports/nv/2nv6 ftp://data.pdbj.org/pub/pdb/validation_reports/nv/2nv6 | HTTPS FTP |
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-Related structure data
Related structure data | 1enzS S: Starting model for refinement |
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Similar structure data |
-Links
-Assembly
Deposited unit |
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1 |
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Unit cell |
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Details | The biological assembly is a tetramer generated from the monomer in the asymmetric unit |
-Components
#1: Protein | Mass: 28377.562 Da / Num. of mol.: 1 / Mutation: D2A, S94A Source method: isolated from a genetically manipulated source Source: (gene. exp.) Mycobacterium tuberculosis (bacteria) / Gene: inhA / Plasmid: pET30b / Species (production host): Escherichia coli / Production host: Escherichia coli BL21(DE3) (bacteria) / Strain (production host): BL21(DE3) References: UniProt: P0A5Y6, UniProt: P9WGR1*PLUS, enoyl-[acyl-carrier-protein] reductase (NADH) |
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#2: Chemical | ChemComp-ZID / |
#3: Water | ChemComp-HOH / |
-Experimental details
-Experiment
Experiment | Method: X-RAY DIFFRACTION / Number of used crystals: 1 |
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-Sample preparation
Crystal | Density Matthews: 3.42 Å3/Da / Density % sol: 64.02 % |
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Crystal grow | Temperature: 289 K / Method: vapor diffusion, hanging drop / pH: 7.5 Details: 12% MPD, 4% DMSO, 0.1 M Hepes, pH 7.5, VAPOR DIFFUSION, HANGING DROP, temperature 289K |
-Data collection
Diffraction | Mean temperature: 121 K |
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Diffraction source | Source: SYNCHROTRON / Site: APS / Beamline: 23-ID-B / Wavelength: 0.97 Å |
Detector | Type: ADSC QUANTUM 315 / Detector: CCD |
Radiation | Protocol: SINGLE WAVELENGTH / Monochromatic (M) / Laue (L): M / Scattering type: x-ray |
Radiation wavelength | Wavelength: 0.97 Å / Relative weight: 1 |
Reflection | Resolution: 1.9→50 Å / Num. obs: 31156 / % possible obs: 97.3 % / Redundancy: 15.1 % / Biso Wilson estimate: 20.3 Å2 / Rsym value: 0.092 / Net I/σ(I): 29.5 |
Reflection shell | Resolution: 1.9→1.97 Å / Redundancy: 9 % / Mean I/σ(I) obs: 1.5 / Num. unique all: 2427 / Rsym value: 0.81 / % possible all: 77.1 |
-Processing
Software |
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Refinement | Method to determine structure: MOLECULAR REPLACEMENT Starting model: PDB ENTRY 1ENZ Resolution: 1.9→33.74 Å / Rfactor Rfree error: 0.004 / Data cutoff high absF: 58202.8 / Data cutoff low absF: 0 / Isotropic thermal model: RESTRAINED / Cross valid method: THROUGHOUT / σ(F): 0
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Solvent computation | Solvent model: FLAT MODEL / Bsol: 40.4826 Å2 / ksol: 0.327175 e/Å3 | ||||||||||||||||||||||||||||||||||||||||||||||||||||||||||||
Displacement parameters | Biso mean: 31.8 Å2
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Refine analyze |
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Refinement step | Cycle: LAST / Resolution: 1.9→33.74 Å
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Refine LS restraints |
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LS refinement shell | Resolution: 1.9→2.02 Å / Rfactor Rfree error: 0.018 / Total num. of bins used: 6
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Xplor file |
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